Cargando…

Pyruvate dehydrogenase kinase 1 promotes neuronal apoptosis upon Japanese encephalitis virus infection

Infection by Japanese Encephalitis Virus (JEV) in humans is primarily characterized by signs and symptoms including non-specific febrile illness, arthralgia, myalgia etc. followed by its resolution due to joint action of host innate and adaptive immunity. However, in selective cases, complications a...

Descripción completa

Detalles Bibliográficos
Autores principales: Chakraborty, Surajit, Sen, Ellora, Basu, Anirban
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795281/
https://www.ncbi.nlm.nih.gov/pubmed/36590093
http://dx.doi.org/10.1016/j.ibneur.2022.10.011
_version_ 1784860224900825088
author Chakraborty, Surajit
Sen, Ellora
Basu, Anirban
author_facet Chakraborty, Surajit
Sen, Ellora
Basu, Anirban
author_sort Chakraborty, Surajit
collection PubMed
description Infection by Japanese Encephalitis Virus (JEV) in humans is primarily characterized by signs and symptoms including non-specific febrile illness, arthralgia, myalgia etc. followed by its resolution due to joint action of host innate and adaptive immunity. However, in selective cases, complications arise owing to invasion of central nervous system (CNS) by JEV. Patients being unable to control peripheral viral replication owing to differences in host genetics and immunity experience JEV-associated neurological complications manifested in the form of headache, nausea, meningoencephalitis, coma and eventual death. Entry of JEV into CNS activates complex cascade of events resulting in loss of neuronal physiology and thus CNS tissue integrity. In present study, we have demonstrated role played by JEV in modulation of neuronal pyruvate dehydrogenase kinase 1 (PDK1) abundance and its effect upon neuronal health. Infection of neuron by JEV culminates into upregulation of PDK1 abundance. Albeit inhibition of JEV-induced PDK1-upregulation was accompanied by enhanced JEV propagation in neurons, abrogation of PDK1-upregulation was demonstrated to ameliorate neuronal apoptosis. PDK1 inhibition-associated reduction in neuronal death was observed to be associated with reduced generation of reactive oxygen species (ROS) in neurons. Our study hence provides a possible therapeutic target which upon modulation might help combat JEV infection-associated neuronal apoptosis via restoration of JEV-associated ROS generation.
format Online
Article
Text
id pubmed-9795281
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-97952812022-12-29 Pyruvate dehydrogenase kinase 1 promotes neuronal apoptosis upon Japanese encephalitis virus infection Chakraborty, Surajit Sen, Ellora Basu, Anirban IBRO Neurosci Rep Articles from the Special Issue Neuroscience in Asia-Pacific; Edited by Wael Mohamed Infection by Japanese Encephalitis Virus (JEV) in humans is primarily characterized by signs and symptoms including non-specific febrile illness, arthralgia, myalgia etc. followed by its resolution due to joint action of host innate and adaptive immunity. However, in selective cases, complications arise owing to invasion of central nervous system (CNS) by JEV. Patients being unable to control peripheral viral replication owing to differences in host genetics and immunity experience JEV-associated neurological complications manifested in the form of headache, nausea, meningoencephalitis, coma and eventual death. Entry of JEV into CNS activates complex cascade of events resulting in loss of neuronal physiology and thus CNS tissue integrity. In present study, we have demonstrated role played by JEV in modulation of neuronal pyruvate dehydrogenase kinase 1 (PDK1) abundance and its effect upon neuronal health. Infection of neuron by JEV culminates into upregulation of PDK1 abundance. Albeit inhibition of JEV-induced PDK1-upregulation was accompanied by enhanced JEV propagation in neurons, abrogation of PDK1-upregulation was demonstrated to ameliorate neuronal apoptosis. PDK1 inhibition-associated reduction in neuronal death was observed to be associated with reduced generation of reactive oxygen species (ROS) in neurons. Our study hence provides a possible therapeutic target which upon modulation might help combat JEV infection-associated neuronal apoptosis via restoration of JEV-associated ROS generation. Elsevier 2022-10-29 /pmc/articles/PMC9795281/ /pubmed/36590093 http://dx.doi.org/10.1016/j.ibneur.2022.10.011 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles from the Special Issue Neuroscience in Asia-Pacific; Edited by Wael Mohamed
Chakraborty, Surajit
Sen, Ellora
Basu, Anirban
Pyruvate dehydrogenase kinase 1 promotes neuronal apoptosis upon Japanese encephalitis virus infection
title Pyruvate dehydrogenase kinase 1 promotes neuronal apoptosis upon Japanese encephalitis virus infection
title_full Pyruvate dehydrogenase kinase 1 promotes neuronal apoptosis upon Japanese encephalitis virus infection
title_fullStr Pyruvate dehydrogenase kinase 1 promotes neuronal apoptosis upon Japanese encephalitis virus infection
title_full_unstemmed Pyruvate dehydrogenase kinase 1 promotes neuronal apoptosis upon Japanese encephalitis virus infection
title_short Pyruvate dehydrogenase kinase 1 promotes neuronal apoptosis upon Japanese encephalitis virus infection
title_sort pyruvate dehydrogenase kinase 1 promotes neuronal apoptosis upon japanese encephalitis virus infection
topic Articles from the Special Issue Neuroscience in Asia-Pacific; Edited by Wael Mohamed
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795281/
https://www.ncbi.nlm.nih.gov/pubmed/36590093
http://dx.doi.org/10.1016/j.ibneur.2022.10.011
work_keys_str_mv AT chakrabortysurajit pyruvatedehydrogenasekinase1promotesneuronalapoptosisuponjapaneseencephalitisvirusinfection
AT senellora pyruvatedehydrogenasekinase1promotesneuronalapoptosisuponjapaneseencephalitisvirusinfection
AT basuanirban pyruvatedehydrogenasekinase1promotesneuronalapoptosisuponjapaneseencephalitisvirusinfection